HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595491Generated: October 29, 2026
Acetic Anhydride → HCID 89689617, compound
https://huagongshe.com/reaction/595491
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 89689645 | HCID 89689645 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 89689617 | HCID 89689617 | — |
Reaction Steps
A solution of tert-butyl 2-(6-(benzo[d]thiazol-6-ylamino)-4-(isopropylamino)pyridin-3-yl)-5-methyloxazol-4-ylcarbamate (Example 106) (20 mg, 0.042 mmol) in Tetrahydrofuran (5 mL) was cooled to 0° C. and treated with NaH (0.042 mmol). Stirred the reaction mixture at 0° C. for 10 min. Added Ac2O (0.042 mmol) to the reaction mixture and stirred at 0° C. for 0.5 h. The reaction mixture was quenched with ice pieces and extracted with ethyl acetate. The organic layer was separated, dried over Na2SO4, filtered and concentrated to afford tert-butyl acetyl(2-(6-(benzo[d]thiazol-6-ylamino)-4-(isopropylamino)pyridin-3-yl)-5-methyloxazol-4-yl)carbamate. LC/MS: Acquity BEH C18 2.1×50 mm, 1.8 micron; Solvent A=0.1% TFA in water; Solvent B=0.1% TFA in ACN; gradient 0-100% B over 2 min; retention time: 0.90 min; LCMS (ES-API), m/z 523.6 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09242976B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-2aa07eed689a440e839a8440c5af4752 |
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| Source note | uspto-grants-2016_01 |
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