HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844235Generated: November 1, 2026
2-Ethyl-3-methoxybenzoyl chloride → INXN-1001
https://huagongshe.com/reaction/1844235
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Ethyl-3-methoxybenzoyl chloride | HCID 22144562 | — |
| Reactant | HCID 57751166 | HCID 57751166 | — |
| Product | INXN-1001 | HCID 57751161 | — |
Reaction Steps
Briefly, benzyl carbazate (compound A) was reacted with pivaldehyde to give (E)-N′-(2,2-dimethyl-propylidene)-hydrazinecarboxylic acid benzyl ester (compound B). Compound B was reacted with (S,S)-2-allyl-2-chloro-3,4-dimethyl-5-phenyl-[1,3,2]oxazasilolidine (Compound C; see Leighton et al., J. Am. Chem. Soc. 125:9596 (2003) and WO 03/074534) to give (R)—N′-(1-tert-butyl-but-3-enyl)-hydrazinecarboxylic acid benzyl ester (compound D). Compound D was reacted with 3,5-dimethyl benzoyl chloride to give (R)—N′-(1-tert-butyl-but-3-enyl)-N′-(3,5-dimethyl-benzoyl)-hydrazinecarboxylic acid benzyl ester (compound B). Compound E was hydrogenated to give (R)-3,5-dimethyl-benzoic acid N-(1-tert-butyl-butyl)-hydrazide (compound F). Compound F was reacted with 2-ethyl-3-methoxybenzoyl chloride to give Compound 1. The crude material was triturated first with ether (2% ethanol) and then with 1:1 hexanes:ether in a fritted glass Büchner funnel. The product was then washed with deionized water with thorough mixing and allowed to dry in air. Compound 1 was isolated as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946294B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-10bd9a63c66f4dabb9fa90e99a2f3fc5 |
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| Source note | uspto-grants-2015_02 |
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