HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611520Generated: October 30, 2026
Benzoyl chloride → HCID 19597444, compound
https://huagongshe.com/reaction/611520
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 19597418 | HCID 19597418 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19597444 | HCID 19597444 | — |
Reaction Steps
Benzoyl chloride (101 mg) in dichloromethane (1.0 ml) was added to a mixture of 4-amino-5-(4-aminophenyl)-7-isopropylpyrrolo[2,3-d]pyrimidine (175 mg), in dichloromethane (7 ml) and triethylamine (73 mg) at 0° C. under nitrogen with stirring. The mixture was stirred at 0° C. for four hours and then allowed to warm up to ambient temperature over one hour. The reaction mixture was stirred at ambient temperature for 18 hours and then quenched by the addition of saturated sodium bicarbonate solution (10 ml) with ice-cooling. The organic layer was separated and the aqueous layer was extracted with ethyl acetate (3×20 ml). The combined organic layers were washed with water, dried and evaporated to give a pale yellow solid which was purified by preparative HPLC to give N-(4-{4-amino-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidin-5-yl}phenyl)-benzamide, m.p. 192-195° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06001839 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-212deeadf2054a3387184f6a4922aa64 |
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| Source note | uspto-grants-1999_12 |
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