Ammonia → HCID 58900223, compound

HRID 642647Notes

Reaction equation

HRID 642647 reaction equation
[F:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:11][C:12]1[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14][CH:13]=1)[C:6]1[C:22](=[O:27])[O:23][C:24](=[O:26])[CH2:25][C:5]2=1.[NH3:28]>>[C:24]([CH2:25][C:5]1[C:4]2[C:8](=[CH:9][CH:10]=[C:2]([F:1])[CH:3]=2)[N:7]([CH2:11][C:12]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14][CH:13]=2)[C:6]=1[C:22]([OH:23])=[O:27])(=[O:26])[NH2:28]

Participants

3

Procedure

6-Fluoro-9-naphthalen-1-ylmethyl-4,9-dihydro-pyrano[3,4-b]indole-1,3-dione (from example 34.1.) was ring opened with ammonia at 22° C. to give the title compound as a white solid. MS: 375.1 ([M−H]−).

Sources & evidence

ORD record
ord-b5b4a2a252624b7ab2cef64004f95263
Source dataset
uspto-grants-2010_04
Patent number
US07696240B2

Reaction notes

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